Academic Journal

Drug survival of biologic agents in patients with psoriatic arthritis from a medical center in southern Taiwan

التفاصيل البيبلوغرافية
العنوان: Drug survival of biologic agents in patients with psoriatic arthritis from a medical center in southern Taiwan
المؤلفون: Yu, Sebastian, Tsao, Yu-Hsiang, Tu, Hung-Pin, Lan, Cheng-Che E.
المصدر: Dermatologica Sinica ; volume 40, issue 1, page 20-27 ; ISSN 1027-8117
بيانات النشر: Medknow
سنة النشر: 2022
الوصف: Background: Psoriasis is a chronic inflammatory disease involving the skin and/or joints. Till 2016, there were five biologic agents for psoriatic arthritis treatment in Taiwan: etanercept, adalimumab, golimumab, ustekinumab, and secukinumab. Although European guidelines recommend tumor necrosis factor-α (TNF-α) inhibitors as the first-line biologic agents for axial disease of psoriatic arthritis, the drug survival of biologic agents in Asian populations remains unclear. Objectives: We investigated 5-year drug survival of biologic agents in patients with psoriatic arthritis. Methods: We used Kaohsiung Medical University Hospital Research Database to evaluate real-world 5-year drug survival of biologic agents for psoriatic arthritis in a medical center from southern Taiwan. Results: The 5-year drug survival rates of ustekinumab, etanercept, and adalimumab were significantly different. Ustekinumab and etanercept showed higher 5-year survival rates for psoriatic disease than adalimumab. Golimumab and secukinumab had a short follow-up time to obtain a conclusive 5-year survival rate. Conclusion: Considering that TNF-α inhibitors are often the first-line biologic agents for psoriatic arthritis in guidelines in western countries, the finding that ustekinumab is superior to TNF-α inhibitor adalimumab in terms of 5-year survival for psoriatic disease may imply that the therapeutic response of biologic agents may differ between different ethnic groups.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.4103/ds.ds_8_22
الاتاحة: https://doi.org/10.4103/ds.ds_8_22
https://journals.lww.com/10.4103/ds.ds_8_22
رقم الانضمام: edsbas.93FDFA7D
قاعدة البيانات: BASE